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临床试验/IRCT20080902001181N4
IRCT20080902001181N4招募中3 期

Comparison of the effect of Agnugol, Cimifugol , Soyagol , vitagnus and EsCitalopram in reducing menopausal symptoms in postmenopausal women

Esfahan University of Medical Sciences0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
200

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
45 years 至 65 years(—)
性别
Female

入选标准

  • Obtaining a score of 5 and above from the MRS questionnaire
  • 12 months or more have passed since menopause
  • Age between 45 and 65 years

排除标准

  • Presence or history of breast and uterine cancer, abnormal vaginal bleeding, liver, kidney, thyroid, depression and known anxiety disorders.
  • Use of progestins, contraceptive pills, GNRH agonists and antagonists
  • Taking drugs that interact with the studied drugs, such as warfarin, tamoxifen, antipsychotics, and dopamine antagonists.

研究者

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